Search results for "Paramagnetism"

showing 10 items of 354 documents

Itinerant Electron Metamagnetism in η-Carbide-Type Compound Co3Mo3C

2010

We report the magnetic properties of the cobalt molybdenum η-carbide-type compounds Co 3 Mo 3 C and Co 3 Mo 3 N. The magnetic susceptibility χ of Co 3 Mo 3 C shows a Curie–Weiss temperature dependence at high temperatures and a broad maximum at around 100 K, whereas that of Co 3 Mo 3 N shows a nearly temperature-independent enhanced Pauli paramagnetic behavior. The absence of a magnetic long-range order was confirmed by the nuclear magnetic resonance technique in both the compounds. As expected from the broad maximum of χ, we observed an itinerant electron metamagnetic transition at around 37 T in Co 3 Mo 3 C.

Curie–Weiss lawMaterials scienceCondensed matter physicsGeneral Physics and Astronomychemistry.chemical_elementMagnetic susceptibilityCarbideCrystallographyParamagnetismchemistryMolybdenumCurie temperatureCobaltMetamagnetismJournal of the Physical Society of Japan
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Geometric, electronic, and magnetic structure ofCo2FeSi: Curie temperature and magnetic moment measurements and calculations

2005

In this work a simple concept was used for a systematic search for materials with high spin polarization. It is based on two semiempirical models. First, the Slater-Pauling rule was used for estimation of the magnetic moment. This model is well supported by electronic structure calculations. The second model was found particularly for ${\mathrm{Co}}_{2}$ based Heusler compounds when comparing their magnetic properties. It turned out that these compounds exhibit seemingly a linear dependence of the Curie temperature as function of the magnetic moment. Stimulated by these models, ${\mathrm{Co}}_{2}\mathrm{FeSi}$ was revisited. The compound was investigated in detail concerning its geometrical…

Curie–Weiss lawMaterials scienceExtended X-ray absorption fine structureCondensed matter physicsMagnetic momentMagnetic structureCondensed Matter PhysicsElectronic Optical and Magnetic MaterialsCondensed Matter::Materials ScienceMagnetizationParamagnetismCurie's lawCurie temperatureCondensed Matter::Strongly Correlated ElectronsPhysical Review B
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On/Off Photoswitching in a Cyanide-Bridged {Fe2Co2} Magnetic Molecular Square

2013

International audience; A repeatable bidirectional paramagnetic ↔ diamagnetic photomagnetic effect has been observed in the cyanide-bridged Fe-Co square complex {[Fe{B(pz)(4)}(CN)(3)](2)[Co(bik)(2)](2)}(ClO(4))(2)*3H(2)O [B(pz)(4) = tetrapyrazolylborate, bik = bis(1-methylimidazol-2-yl)ketone]. Magnetic measurements and low-temperature single-crystal X-ray diffraction experiments have shown that a complete electron transfer from the diamagnetic Fe(II)-Co(III) state to the paramagnetic Fe(III)-Co(II) metastable state is induced by 808 nm laser light irradiation, whereas the diamagnetic state is recovered in an almost quantitative yield under irradiation at 532 nm.

CyanideINDUCED ELECTRON-TRANSFERTRANSITIONSRELAXATION010402 general chemistryPhotochemistry01 natural sciencesBiochemistryCOBALT-IRON CYANIDECatalysisPHOTOINDUCED MAGNETIZATIONParamagnetismchemistry.chemical_compoundElectron transferColloid and Surface ChemistryMetastability[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular BiologyIrradiationALKALI-METAL-IONPRUSSIAN BLUE ANALOGS010405 organic chemistryChemistryRelaxation (NMR)Photomagnetic effectGeneral Chemistry3. Good health0104 chemical sciencesCOSOLID-STATECrystallographyDiamagnetismJournal of the American Chemical Society
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Exchange-transfer in mixed-valence clusters with one migrating hole

1996

Abstract A new mechanism for exchange-transfer specific to hole-type mixed-valence clusters is proposed. The intermediate state in the second-order exchange-transfer process is achieved by the jump of the electron from the spin-core of the dn+1 ion into the empty orbital of the dn ion. As distinguished from the mixed-valence clusters with one delocalized electron this intermediate state is the high-spin one giving rise to a ferromagnetic contribution to the ground manifold. On the basis of angular momentum theory a general solution of the exchange-transfer problem is given for arbitrary nuclearity mixed-valence hole-type clusters with many-electron paramagnetic spin-cores. The interplay bet…

Delocalized electronParamagnetismAngular momentumValence (chemistry)FerromagnetismChemistryGeneral Physics and AstronomyIntermediate stateCondensed Matter::Strongly Correlated ElectronsElectronPhysical and Theoretical ChemistryAtomic physicsIonChemical Physics Letters
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ChemInform Abstract: Spin Density Distribution in Transition Metal Complexes: Some Thoughts and Hints

2010

Abstract The spin density distribution in transition metal complexes is discussed in qualitative terms, taking into account the coexistence of spin delocalization and spin polarization mechanisms, with the help of numerical results for several complexes obtained from density functional calculations. The covalent character of the metal-ligand bonds as well as the σ- or π-characteristics of the partially filled d orbitals must be taken into account to qualitatively predict the sign of the spin density at a particular atom within a ligand. The same patterns can be applied to binuclear complexes and can be helpful in determining the ferro- or antiferromagnetic character of the exchange coupling…

Delocalized electronParamagnetismCondensed matter physicsAtomic orbitalTransition metalSpin polarizationChemistryAntiferromagnetismCondensed Matter::Strongly Correlated ElectronsMolecular orbitalGeneral MedicineSpin-½ChemInform
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High-dimensional mixed-valence copper cyanide complexes: Syntheses, structural characterizations and magnetism

2009

International audience; Reactions of CuCl 2 with different CN complexes in presence of a neutral ancillary ligand lead to two novel mixed-valence Cu complexes [Cu II (bpy)Cu I (CN) 3 ] n , 1 (bpy=2,2′-bipyridine) and {[Cu II (tn) 2 ][Cu I 4 (CN) 6 ]} n 2 (tn=1,3-diaminopropane). For compound 1, the asymmetric unit involves two Cu ions Cu1 and Cu2 (Cu I and Cu II centres, respectively) which strongly differ in their environments. The Cu1 ion presents a CuC 4 pseudo-tetrahedral geometry, while the Cu2 ion presents a CuN 5 slightly distorted square-pyramidal geometry. The extended structure of 1 is generated by three cyano ligands which differ in their coordination modes. One CN group has a μ …

DenticityMagnetismInorganic chemistrychemistry.chemical_element[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistry01 natural sciencesCoordination modesIonInorganic ChemistryParamagnetismMagnetic propertiesMaterials ChemistryMixed-valence[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical ChemistryValence (chemistry)Bridging ligands010405 organic chemistryLigand[CHIM.ORGA]Chemical Sciences/Organic chemistryCopper0104 chemical sciencesCrystallographyCopper cyanideschemistryCN-group
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Field-induced single ion magnet behaviour of discrete and one-dimensional complexes containing [bis(1-methylimidazol-2-yl)ketone]-cobalt(II) building…

2021

International audience; We describe herein the first examples of six-coordinate CoII single-ion magnets (SIMs) based on the β-diimine Mebik ligand [Mebik = bis(1-methylimidazol-2-yl)ketone]: two mononuclear [CoII(Rbik)2L2] complexes and one mixed-valence {CoIII2CoII}n chain of formulas [CoII(Mebik)(H2O)(dmso)(μ-NC)2CoIII2(μ-2,5-dpp)(CN)6]n·1.4nH2O (3) [L = NCS (1), NCSe (2) and 2,5-dpp = 2,5-bis(2-pyridyl)pyrazine (3)]. Two bidentate Mebik molecules plus two monodentate N-coordinated pseudohalide groups in cis positions build somewhat distorted octahedral surroundings around the high-spin cobalt(II) ions in 1 and 2. The diamagnetic [CoIII2(μ-2,5-dpp)(CN)8]2− metalloligand coordinates the pa…

DenticityMaterials sciencePyrazine010405 organic chemistrychemistry.chemical_element010402 general chemistry01 natural sciences0104 chemical scienceslaw.inventionInorganic ChemistryMagnetizationCrystallographyParamagnetismMagnetic anisotropychemistry.chemical_compoundchemistrylaw[CHIM]Chemical SciencesMoleculeElectron paramagnetic resonanceCobaltDalton transactions (Cambridge, England : 2003)
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Method and apparatus using selected superparamagnetic labels for rapid quantification of immunochromatographic tests

2009

Mika PA Laitinen1, Jari Salmela2, Leona Gilbert1, Risto Kaivola1, Topi Tikkala2, Christian Oker-Blom1, Jukka Pekola3, Matti Vuento11Department of Biological and Environmental Science; 2Department of Physics, University of Jyväskylä, Jyväskylä, Finland; 3Low Temperature Laboratory, Helsinki University of Technology, Helsinki, FinlandAbstract: A rapid method and instrumentation for quantification of immunochromatographic tests (ICT) are described. The principle and performance of the method was demonstrated by measuring the levels of human chorionic gonadotropin (hCG) present in urine. The test format was a sandwich assay using two distinct monoclonal antib…

Detection limitAnalyteendocrine systemChromatographyChemistryCapillary actionmedicine.drug_classBiomedical EngineeringBioengineeringBioinformaticsMonoclonal antibodyLinear rangemedicineUrine sampleBiosensorhormones hormone substitutes and hormone antagonistsSuperparamagnetismOriginal ResearchNanotechnology Science and ApplicationsNanotechnology, Science and Applications
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Multifunctional two-photon active silica-coated Au@MnO Janus particles for selective dual functionalization and imaging.

2014

Monodisperse multifunctional and nontoxic Au@MnO Janus particles with different sizes and morphologies were prepared by a seed-mediated nucleation and growth technique with precise control over domain sizes, surface functionalization, and dye labeling. The metal oxide domain could be coated selectively with a thin silica layer, leaving the metal domain untouched. In particular, size and morphology of the individual (metal and metal oxide) domains could be controlled by adjustment of the synthetic parameters. The SiO2 coating of the oxide domain allows biomolecule conjugation (e.g., antibodies, proteins) in a single step for converting the photoluminescent and superparamagnetic Janus nanopar…

Diagnostic ImagingCell SurvivalSurface PropertiesDispersityOxideMetal NanoparticlesJanus particlesNanotechnologyBiochemistryCatalysischemistry.chemical_compoundColloid and Surface ChemistryMicroscopy Electron TransmissionCell Line TumorMicroscopySpectroscopy Fourier Transform InfraredHumansParticle SizePhotonsChemistryBiological TransportGeneral ChemistrySilicon DioxideTransmission electron microscopySurface modificationNanoparticlesParticle sizeGoldSuperparamagnetismHeLa CellsJournal of the American Chemical Society
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The Crystal Structure of Nickel(II)-Azurin

1995

The nickel(II)-azurin metalloderivative has been crystallized and its structure solved at 0.205-nm resolution by X-ray diffraction. The overall structure is not modified by the metal exchange and the only differences with regard to the native copper(II)-azurin occur in the metal site region. These variations affect principally the axial ligands. Nickel co-ordinates more strongly to the carbonyl oxygen of Gly45 while its distance to the Met121 S4 enlarges up to 0.330 nm. The resulting metal center structure is intermediate between those of the Cu(II) and Zn(II) azurins, and can be described as distorted tetrahedral. However, the existence of contact interaction between Met121 and the nickel …

DiffractionMagnetic Resonance SpectroscopyMolecular Structurechemistry.chemical_elementCrystal structureCrystallography X-RayOxygenBiochemistryMetalCrystallographyParamagnetismNickelchemistryAzurinNickelvisual_artX-ray crystallographyvisual_art.visual_art_mediumAzurinEuropean Journal of Biochemistry
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